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Regulatory Forum for Medical Devices

August 7, 2017

Date: December 5th and 6th of 2016.

Location: Laboratorios Scantibodies

Description: 1st edition of the Forum COFEPRIS for the Medical Products Industry, the objective is to establish an agreement to recognize the normativity applicable to Medical Devices, in order to comply with the requirements that must be accredited to obtain a registration in “Sanitary Conditions” or modifications to the “Sanitary Conditions”. The process of obtaining the Certificate of Good Manufacturing Practices was identified and the guidelines of the Technovigilance were known for the preparation of the corresponding report.





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